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CN105210874B - A kind of blueberry method for culturing seedlings - Google Patents

A kind of blueberry method for culturing seedlings Download PDF

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CN105210874B
CN105210874B CN201510671296.4A CN201510671296A CN105210874B CN 105210874 B CN105210874 B CN 105210874B CN 201510671296 A CN201510671296 A CN 201510671296A CN 105210874 B CN105210874 B CN 105210874B
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blueberry
root
cuttage
culture
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卢政锋
尹静瑶
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Daxinganling Lvfeng Forest Economic Technology Development Co.,Ltd.
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TONGREN MCKINNON GREEN AGRICULTURE TECHNOLOGY Co Ltd
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Abstract

The present invention relates to blueberry seedling-raising technique fields, especially a kind of blueberry method for culturing seedlings, by by semi-lignified branch segment, detergent immersion, sodium hypochlorite impregnate, mercuric chloride solution impregnates, flushing is seeded in WPM culture mediums repeatedly, and carry out improved treatment to WPM culture mediums so that the interaction between its nutritional ingredient is adjusted, and then while nutritional ingredient is provided in for blueberry seedling raising process, also promote the growth of blueberry twig and improving quality, improve premunition, reduce blueberry seedling cost;In conjunction with being cultivated in switching root media so that blueberry root system is quickly flourishing, and ensures the survival rate of follow-up blueberry transplanting, reduces production cost.

Description

一种蓝莓育苗方法A kind of blueberry seedling raising method

技术领域technical field

本发明涉及蓝莓育苗技术领域,尤其是一种蓝莓育苗方法。The invention relates to the technical field of blueberry seedling cultivation, in particular to a blueberry seedling cultivation method.

背景技术Background technique

蓝莓(Blueberry),意为蓝色的浆果之意。其根据培育的方式不同以及蓝莓生长的环境不同,其呈现出来的特征也是不相同的,进而被分为两种类型,一种是低灌木,矮脚野生,颗粒小,但花青素的含量很高的品种,另外一种是人工培育的,能成长至240cm高,果实较大,水分较多,花青素含量相对偏低的品种。蓝莓果实中含有丰富的营养成分,它不仅具有良好的营养保健作用,还具有防止脑神经老化、强心、抗癌软化血管、增强人机体免疫等功能。尤其是蓝莓中的花青素,其能够抗衰老、抗氧化,提高人体免疫力。Blueberry (Blueberry), means the meaning of blue berry. According to the different cultivation methods and the different growth environments of blueberries, the characteristics they present are also different, and they are further divided into two types, one is low shrub, short-footed wild, small particles, but the content of anthocyanins The tall variety, the other is artificially bred, can grow to 240cm high, has larger fruit, more water, and a relatively low anthocyanin content. Blueberry fruit is rich in nutrients. It not only has good nutritional and health effects, but also has the functions of preventing brain aging, strengthening the heart, anti-cancer, softening blood vessels, and enhancing human immunity. Especially the anthocyanins in blueberries, which can resist aging, resist oxidation and improve human immunity.

但是,随着蓝莓的需求量不断的增大和产业的不断发展,对于蓝莓的需求量也越来越多,为此,野生蓝莓的供给再也不能满足蓝莓产业的需求了,而人工培育蓝莓又会造成蓝莓中花青素含量大幅度的降低,进而影响蓝莓产业的健康发展。But, along with the continuous increase of the demand of blueberry and the continuous development of industry, also more and more for the demand of blueberry, for this reason, the supply of wild blueberry can no longer meet the demand of blueberry industry, and artificially cultivated blueberry and It will cause a significant reduction in the anthocyanin content in blueberries, which in turn will affect the healthy development of the blueberry industry.

于是,如何提供一种人工育苗,降低蓝莓品种变异的缺陷成为了蓝莓产业快速、健康发展的制约因素之一。而现有技术中,大量的研究者也从事了蓝莓苗育苗方法的研究和处理,并且也取得了一定的突破和发展,但是,其培育出来的蓝莓苗的品质依然较差,变异程度依然较大,并且其培育的周期还相对较长,培育后的蓝莓苗移栽的成活率较低,使得蓝莓种植的成本较高,阻碍了蓝莓产业的快速、健康发展。Therefore, how to provide a kind of artificial seedling cultivation and reduce the defects of blueberry variety variation has become one of the restrictive factors for the rapid and healthy development of the blueberry industry. And in the prior art, a large amount of researchers have also been engaged in the research and processing of blueberry seedling raising method, and also obtained certain breakthrough and development, but, the quality of the blueberry seedling that it cultivates is still relatively poor, and the degree of variation is still relatively high. Large, and its cultivation cycle is relatively long, the survival rate of transplanted blueberry seedlings after cultivation is low, which makes the cost of blueberry planting higher and hinders the rapid and healthy development of the blueberry industry.

发明内容Contents of the invention

为了解决现有技术中存在的上述技术问题,本发明提供一种蓝莓育苗方法。In order to solve the above-mentioned technical problems existing in the prior art, the present invention provides a method for growing blueberry seedlings.

具体是通过以下技术方案得以实现的:Specifically, it is achieved through the following technical solutions:

一种蓝莓育苗方法,包括以下步骤:A method for raising blueberry seedlings, comprising the following steps:

(1)选择半木质化枝条,将其切成1-1.5cm的单芽枝段,采用饱和洗衣粉水浸泡9-11min,再用自来水冲洗9-11min,再在无菌条件下,采用质量浓度为70%的次氯酸钠浸泡4-6min后,再用质量浓度为0.1%的升汞溶液浸泡7-9min,再用无菌水反复冲洗5-6次,再将其接种在WPM培养基上培养,控制温度为24-26℃,光照强度为1900-2100LX,光照时间为15-17h/天;(1) Select semi-lignified branches, cut them into 1-1.5cm single-bud branches, soak them in saturated washing powder water for 9-11 minutes, then rinse them with tap water for 9-11 minutes, and then use quality Soak in 70% sodium hypochlorite for 4-6 minutes, then soak in 0.1% mercuric chloride solution for 7-9 minutes, then rinse with sterile water for 5-6 times, then inoculate it on WPM medium for cultivation , the control temperature is 24-26°C, the light intensity is 1900-2100LX, and the light time is 15-17h/day;

(2)待步骤1)培养至植株长至株高为6-8cm后,并将其转接生根培养基中进行生根处理,即可。(2) After step 1) is cultivated until the plant grows to a plant height of 6-8cm, it is transferred to the rooting medium for rooting treatment.

所述的生根处理为瓶外扦插生根培养或瓶内培养生根。The rooting treatment is the rooting culture of cuttings outside the bottle or the rooting culture in the bottle.

所述的瓶外扦插生根培养是将株高为6-8cm的植株剪切成3-5cm的扦插条,并将扦插条扦插在生根培养基上,扦插深度为1-1.5cm,并在扦插前采用质量体积浓度为0.1mg/L的IBA浸沾,并在扦插后,控制温度为24-26℃,光照强度1000-2000K、光照时间为15-17h/天,培养两个月,即可。The rooting culture of cuttings outside the bottle is to cut the plants with a plant height of 6-8cm into cutting strips of 3-5cm, and cut the cutting strips on the rooting medium, the cutting depth is 1-1.5cm, and cut the cutting strips on the rooting medium. Use IBA with a mass volume concentration of 0.1mg/L before dipping, and after cuttings, control the temperature at 24-26°C, light intensity 1000-2000K, light time 15-17h/day, and cultivate for two months. .

所述的瓶内培养生根是将株高为6-8cm的植株转接在生根培养基中,其中生根培养基是盛装在广口瓶中,其生根培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L,再将其置于温度为24-26℃、光照强度为1000-2000K、光照时间为15-17h/天,培养两个月,即可。The cultivation rooting in described bottle is that the plant height of 6-8cm is transferred in the rooting medium, wherein the rooting medium is contained in a jar, and its rooting medium is 1/2WPM medium adding IBA, Make the concentration of IBA in the culture medium 0.1mg/L, then place it at a temperature of 24-26°C, light intensity of 1000-2000K, light time of 15-17h/day, and cultivate for two months.

所述的生根培养基为瓶外扦插生根培养基,其组成为泥炭土和树皮粉按照质量比为3∶1进行混合均匀的混合物。The rooting medium is a rooting medium for cuttings outside a bottle, which is composed of peat soil and bark powder uniformly mixed in a mass ratio of 3:1.

所述的生根培养基为瓶内培养生根培养基,该培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L。Described rooting medium is culture rooting medium in the bottle, and this medium is 1/2WPM medium and adds IBA, makes the concentration of IBA in the medium be 0.1mg/L.

所述的WPM培养基,以每升计,其原料成分为硝酸铵400mg、硝酸钙556mg、硫酸钾990mg、氯化钙96mg、磷酸二氢钾170mg、钼酸钠0.25mg、硫酸镁370mg、硫酸锰22.4mg、硫酸锌8.6mg、硫酸铜0.25mg、硫酸亚铁27.8mg、Na2-EDTA37.3mg、肌醇100mg、烟酸0.5mg、维生素B60.5mg、甘氨酸2.0mg、蔗糖20g、琼脂6g、玉米素0.5~1mg。Described WPM culture medium, by every liter, its raw material composition is ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, sulfate Manganese 22.4mg, Zinc Sulfate 8.6mg, Copper Sulfate 0.25mg, Ferrous Sulfate 27.8mg, Na 2 -EDTA 37.3mg, Inositol 100mg, Niacin 0.5mg, Vitamin B6 0.5mg, Glycine 2.0mg, Sucrose 20g, Agar 6g , Zeatin 0.5 ~ 1mg.

所述的无菌水为蒸馏水或自来水被80-100℃煮10-30min后冷却至常温的冷却水。The sterile water is distilled water or tap water boiled at 80-100° C. for 10-30 minutes and then cooled to normal temperature.

与现有技术相比,其技术效果体现在:Compared with the existing technology, its technical effect is reflected in:

通过将半木质化枝条切段,洗衣粉浸泡、次氯酸钠浸泡、升汞溶液浸泡、反复冲洗接种在WPM培养基,并对WPM培养基进行改良处理,使得其营养成分之间的相互作用得到调整,进而在为蓝莓育苗过程中提供营养成分的同时,还促进蓝莓枝芽生长以及改善品质,提高抗病力,降低蓝莓育苗成本;再结合转接生根培养基中进行培养,使得蓝莓根系快速发达,并确保了后续蓝莓移栽的成活率,降低了生产成本。By cutting the semi-lignified branches, soaking them in washing powder, sodium hypochlorite, mercuric solution, washing repeatedly and inoculating them on the WPM medium, and improving the WPM medium, the interaction between the nutrients can be adjusted. Furthermore, while providing nutrients for the blueberry seedling cultivation process, it also promotes the growth of blueberry shoots and improves the quality, improves disease resistance, and reduces the cost of blueberry seedling cultivation; combined with the cultivation in the transfer rooting medium, the blueberry root system develops rapidly. And the survival rate of subsequent blueberry transplanting is ensured, and the production cost is reduced.

本发明尤其是将蓝莓根系的培养以及蓝莓苗植株体的培养经过不同的培养基进行,进而确保根系生长所需的营养物质不被植株体生长所需的营养物质影响,进而改善了蓝莓苗生长环境,提高了蓝莓的品质,进而降低蓝莓的发病率;尤其是经过生根培养基的培养,不仅使得蓝莓根系发达,抗病力增强,而且使得蓝莓苗老化、成熟,进而提高适应环境的能力,降低移栽损失率,提高了成活率。In particular, the present invention carries out the cultivation of the blueberry root system and the cultivation of the blueberry seedling plant body through different mediums, thereby ensuring that the nutrients required for root growth are not affected by the nutrients required for plant body growth, thereby improving the growth of blueberry seedlings environment, improve the quality of blueberries, and then reduce the incidence of blueberries; especially through the cultivation of rooting medium, not only makes the blueberry root system developed, the disease resistance is enhanced, but also makes the blueberry seedlings aging and mature, thereby improving the ability to adapt to the environment, Reduce the loss rate of transplanting and improve the survival rate.

具体实施方式Detailed ways

下面结合具体的实施方式来对本发明的技术方案做进一步的限定,但要求保护的范围不仅局限于所作的描述。The technical solutions of the present invention will be further limited below in conjunction with specific embodiments, but the scope of protection is not limited to the descriptions made.

实施例1Example 1

一种蓝莓育苗方法,包括以下步骤:A method for raising blueberry seedlings, comprising the following steps:

(1)选择半木质化枝条,将其切成1cm的单芽枝段,采用饱和洗衣粉水浸泡9min,再用自来水冲洗9min,再在无菌条件下,采用质量浓度为70%的次氯酸钠浸泡4min后,再用质量浓度为0.1%的升汞溶液浸泡7min,再用无菌水反复冲洗5次,再将其接种在WPM培养基上培养,控制温度为24℃,光照强度为1900LX,光照时间为15h/天;(1) Select semi-lignified branches, cut them into 1cm single-bud branches, soak them in saturated washing powder water for 9 minutes, then rinse them with tap water for 9 minutes, and then soak them in 70% sodium hypochlorite under aseptic conditions. After 4 minutes, soak in mercuric chloride solution with a mass concentration of 0.1% for 7 minutes, rinse repeatedly with sterile water for 5 times, and then inoculate it on WPM medium for cultivation. The time is 15h/day;

(2)待步骤1)培养至植株长至株高为6cm后,并将其转接生根培养基中进行生根处理,即可。(2) After the step 1) is cultivated until the plant grows to a plant height of 6 cm, it is transferred to the rooting medium for rooting treatment.

所述的生根处理为瓶外扦插生根培养。The rooting treatment is rooting culture of cuttings outside the bottle.

所述的瓶外扦插生根培养是将株高为6cm的植株剪切成3cm的扦插条,并将扦插条扦插在生根培养基上,扦插深度为1cm,并在扦插前采用质量体积浓度为0.1mg/L的IBA浸沾,并在扦插后,控制温度为24℃,光照强度1000K、光照时间为15h/天,培养两个月,即可。The rooting culture of cuttings outside the bottle is to cut the plants with a plant height of 6cm into 3cm cutting strips, and cut the cutting strips on the rooting medium, the cutting depth is 1cm, and the mass volume concentration is 0.1 before cutting. mg/L IBA, and after cuttings, control the temperature at 24°C, light intensity 1000K, light time 15h/day, and cultivate for two months.

所述的生根培养基为瓶外扦插生根培养基,其组成为泥炭土和树皮粉按照质量比为3∶1进行混合均匀的混合物。The rooting medium is a rooting medium for cuttings outside a bottle, which is composed of peat soil and bark powder uniformly mixed in a mass ratio of 3:1.

所述的WPM培养基,以每升计,其原料成分为硝酸铵400mg、硝酸钙556mg、硫酸钾990mg、氯化钙96mg、磷酸二氢钾170mg、钼酸钠0.25mg、硫酸镁370mg、硫酸锰22.4mg、硫酸锌8.6mg、硫酸铜0.25mg、硫酸亚铁27.8mg、Na2-EDTA37.3mg、肌醇100mg、烟酸0.5mg、维生素B60.5mg、甘氨酸2.0mg、蔗糖20g、琼脂6g、玉米素0.5mg。Described WPM culture medium, by every liter, its raw material composition is ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, sulfate Manganese 22.4mg, Zinc Sulfate 8.6mg, Copper Sulfate 0.25mg, Ferrous Sulfate 27.8mg, Na 2 -EDTA 37.3mg, Inositol 100mg, Niacin 0.5mg, Vitamin B6 0.5mg, Glycine 2.0mg, Sucrose 20g, Agar 6g , Zeatin 0.5mg.

所述的无菌水为自来水被80℃煮10min后冷却至常温的冷却水。The sterile water is cooling water that is boiled at 80° C. for 10 minutes and then cooled to normal temperature.

实施例2Example 2

一种蓝莓育苗方法,包括以下步骤:A method for raising blueberry seedlings, comprising the following steps:

(1)选择半木质化枝条,将其切成1.5cm的单芽枝段,采用饱和洗衣粉水浸泡11min,再用自来水冲洗11min,再在无菌条件下,采用质量浓度为70%的次氯酸钠浸泡6min后,再用质量浓度为0.1%的升汞溶液浸泡9min,再用无菌水反复冲洗6次,再将其接种在WPM培养基上培养,控制温度为26℃,光照强度为2100LX,光照时间为17h/天;(1) Select semi-lignified branches, cut them into 1.5cm single-bud branches, soak them in saturated washing powder water for 11 minutes, then rinse them with tap water for 11 minutes, and then use 70% sodium hypochlorite under aseptic conditions After soaking for 6 minutes, soak in mercuric chloride solution with a mass concentration of 0.1% for 9 minutes, then rinse with sterile water for 6 times, then inoculate it on WPM medium for cultivation, control the temperature at 26°C, and light intensity at 2100LX. The light time is 17h/day;

(2)待步骤1)培养至植株长至株高为8cm后,并将其转接生根培养基中进行生根处理,即可。(2) After step 1) is cultivated until the plant grows to a plant height of 8 cm, it is transferred to the rooting medium for rooting treatment.

所述的生根处理为瓶内培养生根。Described rooting process is culture rooting in the bottle.

所述的瓶内培养生根是将株高为8cm的植株转接在生根培养基中,其中生根培养基是盛装在广口瓶中,其生根培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L,再将其置于温度为26℃、光照强度为2000K、光照时间为17h/天,培养两个月,即可。The cultivation rooting in described bottle is that the plant height of 8cm is transferred in the rooting medium, wherein the rooting medium is contained in a wide-mouth bottle, and its rooting medium is 1/2WPM medium adding IBA, so that IBA The concentration in the culture medium is 0.1mg/L, and then it is placed at a temperature of 26°C, a light intensity of 2000K, and a light time of 17h/day, and cultured for two months.

所述的生根培养基为瓶内培养生根培养基,该培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L。Described rooting medium is culture rooting medium in the bottle, and this medium is 1/2WPM medium and adds IBA, makes the concentration of IBA in the medium be 0.1mg/L.

所述的WPM培养基,以每升计,其原料成分为硝酸铵400mg、硝酸钙556mg、硫酸钾990mg、氯化钙96mg、磷酸二氢钾170mg、钼酸钠0.25mg、硫酸镁370mg、硫酸锰22.4mg、硫酸锌8.6mg、硫酸铜0.25mg、硫酸亚铁27.8mg、Na2-EDTA37.3mg、肌醇100mg、烟酸0.5mg、维生素B60.5mg、甘氨酸2.0mg、蔗糖20g、琼脂6g、玉米素1mg。Described WPM culture medium, by every liter, its raw material composition is ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, sulfate Manganese 22.4mg, Zinc Sulfate 8.6mg, Copper Sulfate 0.25mg, Ferrous Sulfate 27.8mg, Na 2 -EDTA 37.3mg, Inositol 100mg, Niacin 0.5mg, Vitamin B6 0.5mg, Glycine 2.0mg, Sucrose 20g, Agar 6g , Zeatin 1mg.

所述的无菌水为自来水被100℃煮30min后冷却至常温的冷却水。The sterile water is tap water boiled at 100° C. for 30 minutes and then cooled to normal temperature.

实施例3Example 3

一种蓝莓育苗方法,包括以下步骤:A method for raising blueberry seedlings, comprising the following steps:

(1)选择半木质化枝条,将其切成1.3cm的单芽枝段,采用饱和洗衣粉水浸泡10min,再用自来水冲洗10min,再在无菌条件下,采用质量浓度为70%的次氯酸钠浸泡5min后,再用质量浓度为0.1%的升汞溶液浸泡8min,再用无菌水反复冲洗5次,再将其接种在WPM培养基上培养,控制温度为25℃,光照强度为2000LX,光照时间为16h/天;(1) Select semi-lignified branches, cut them into 1.3cm single-bud branches, soak them in saturated washing powder water for 10 minutes, rinse them with tap water for 10 minutes, and then use 70% sodium hypochlorite under aseptic conditions After soaking for 5 minutes, soak in mercuric chloride solution with a mass concentration of 0.1% for 8 minutes, rinse repeatedly with sterile water for 5 times, then inoculate it on WPM medium for cultivation, control the temperature at 25°C, and light intensity at 2000LX. The light time is 16h/day;

(2)待步骤1)培养至植株长至株高为7cm后,并将其转接生根培养基中进行生根处理,即可。(2) After step 1) is cultivated until the plant grows to a plant height of 7 cm, it is transferred to the rooting medium for rooting treatment.

所述的生根处理为瓶外扦插生根培养。The rooting treatment is rooting culture of cuttings outside the bottle.

所述的瓶外扦插生根培养是将株高为7cm的植株剪切成4cm的扦插条,并将扦插条扦插在生根培养基上,扦插深度为1.3cm,并在扦插前采用质量体积浓度为0.1mg/L的IBA浸沾,并在扦插后,控制温度为25℃,光照强度1500K、光照时间为16h/天,培养两个月,即可。The rooting culture of cuttings outside the bottle is to cut the plants with a plant height of 7cm into 4cm cutting strips, and cut the cutting strips on the rooting medium, the cutting depth is 1.3cm, and before cutting, the mass volume concentration is Soak with 0.1mg/L IBA, and after cuttings, control the temperature at 25°C, light intensity at 1500K, light time at 16h/day, and cultivate for two months.

所述的生根培养基为瓶外扦插生根培养基,其组成为泥炭土和树皮粉按照质量比为3∶1进行混合均匀的混合物。The rooting medium is a rooting medium for cuttings outside a bottle, which is composed of peat soil and bark powder uniformly mixed in a mass ratio of 3:1.

所述的WPM培养基,以每升计,其原料成分为硝酸铵400mg、硝酸钙556mg、硫酸钾990mg、氯化钙96mg、磷酸二氢钾170mg、钼酸钠0.25mg、硫酸镁370mg、硫酸锰22.4mg、硫酸锌8.6mg、硫酸铜0.25mg、硫酸亚铁27.8mg、Na2-EDTA37.3mg、肌醇100mg、烟酸0.5mg、维生素B60.5mg、甘氨酸2.0mg、蔗糖20g、琼脂6g、玉米素0.8mg。Described WPM culture medium, by every liter, its raw material composition is ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, sulfate Manganese 22.4mg, Zinc Sulfate 8.6mg, Copper Sulfate 0.25mg, Ferrous Sulfate 27.8mg, Na 2 -EDTA 37.3mg, Inositol 100mg, Niacin 0.5mg, Vitamin B6 0.5mg, Glycine 2.0mg, Sucrose 20g, Agar 6g , Zeatin 0.8mg.

所述的无菌水为自来水被90℃煮20min后冷却至常温的冷却水。The sterile water is tap water boiled at 90°C for 20 minutes and then cooled to normal temperature.

实施例4Example 4

一种蓝莓育苗方法,包括以下步骤:A method for raising blueberry seedlings, comprising the following steps:

(1)选择半木质化枝条,将其切成1.2cm的单芽枝段,采用饱和洗衣粉水浸泡11min,再用自来水冲洗9min,再在无菌条件下,采用质量浓度为70%的次氯酸钠浸泡6min后,再用质量浓度为0.1%的升汞溶液浸泡7min,再用无菌水反复冲洗5次,再将其接种在WPM培养基上培养,控制温度为24℃,光照强度为1900LX,光照时间为17h/天;(1) Select semi-lignified branches, cut them into 1.2cm single-bud branches, soak them in saturated washing powder water for 11 minutes, then rinse them with tap water for 9 minutes, and then use 70% sodium hypochlorite under aseptic conditions After soaking for 6 minutes, soak in mercuric chloride solution with a mass concentration of 0.1% for 7 minutes, then rinse with sterile water for 5 times, and then inoculate it on WPM medium for cultivation. The temperature is controlled at 24°C, and the light intensity is 1900LX. The light time is 17h/day;

(2)待步骤1)培养至植株长至株高为7cm后,并将其转接生根培养基中进行生根处理,即可。(2) After step 1) is cultivated until the plant grows to a plant height of 7 cm, it is transferred to the rooting medium for rooting treatment.

所述的生根处理为瓶内培养生根。Described rooting process is culture rooting in the bottle.

所述的瓶内培养生根是将株高为7cm的植株转接在生根培养基中,其中生根培养基是盛装在广口瓶中,其生根培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L,再将其置于温度为25℃、光照强度为1500K、光照时间为16h/天,培养两个月,即可。The cultivation rooting in described bottle is that the plant height of 7cm is transferred in the rooting medium, wherein the rooting medium is contained in a wide-mouth bottle, and its rooting medium is 1/2WPM medium adding IBA, so that IBA The concentration in the culture medium is 0.1mg/L, and then it is placed at a temperature of 25°C, a light intensity of 1500K, and a light time of 16h/day, and cultured for two months.

所述的生根培养基为瓶内培养生根培养基,该培养基为1/2WPM培养基添加IBA,使得IBA在培养基中的浓度为0.1mg/L。Described rooting medium is culture rooting medium in the bottle, and this medium is 1/2WPM medium and adds IBA, makes the concentration of IBA in the medium be 0.1mg/L.

所述的WPM培养基,以每升计,其原料成分为硝酸铵400mg、硝酸钙556mg、硫酸钾990mg、氯化钙96mg、磷酸二氢钾170mg、钼酸钠0.25mg、硫酸镁370mg、硫酸锰22.4mg、硫酸锌8.6mg、硫酸铜0.25mg、硫酸亚铁27.8mg、Na2-EDTA37.3mg、肌醇100mg、烟酸0.5mg、维生素B60.5mg、甘氨酸2.0mg、蔗糖20g、琼脂6g、玉米素0.9mg。Described WPM culture medium, by every liter, its raw material composition is ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, sulfate Manganese 22.4mg, Zinc Sulfate 8.6mg, Copper Sulfate 0.25mg, Ferrous Sulfate 27.8mg, Na 2 -EDTA 37.3mg, Inositol 100mg, Niacin 0.5mg, Vitamin B6 0.5mg, Glycine 2.0mg, Sucrose 20g, Agar 6g , Zeatin 0.9mg.

所述的无菌水为蒸馏水。Described sterile water is distilled water.

Claims (3)

1. a kind of blueberry method for culturing seedlings, which is characterized in that comprise the following steps:
(1) semi-lignified branch is selected, the simple bud branch section of 1-1.5cm is cut into, 9- is impregnated using saturation washing powder water 11min, then 9-11min is rinsed with tap water, then aseptically, mass concentration is used to impregnate 4- for 70% sodium hypochlorite After 6min, then with the mercuric chloride solution that mass concentration is 0.1% impregnate 7-9min, then rinsed 5-6 times repeatedly with sterile water, then by its It is seeded on WPM culture mediums and cultivates, controlled at 24-26 DEG C, intensity of illumination 1900-2100LX, light application time 15- 17h/ days;
(2) cultivate and grown to plant to plant height for after 6-8cm after step 1), and place of taking root is carried out in root media of being transferred Reason, you can;
The WPM culture mediums, in terms of every liter, material composition for ammonium nitrate 400mg, calcium nitrate 556mg, potassium sulfate 990mg, Calcium chloride 96mg, potassium dihydrogen phosphate 170mg, sodium molybdate 0.25mg, magnesium sulfate 370mg, manganese sulfate 22.4mg, zinc sulfate 8.6mg, Copper sulphate 0.25mg, ferrous sulfate 27.8mg, Na2- EDTA37.3mg, inositol 100mg, niacin 0.5mg, vitamin B6 0.5mg、 Glycine 2.0mg, sucrose 20g, agar 6g, 0.5~1mg of zeatin;The rooting treatment for the outer cuttage root-taking culture of bottle or Culture in glassware is taken root;
The outer cuttage root-taking culture of the bottle is that the plant that plant height is 6-8cm is cut into the cuttage item of 3-5cm, and by cuttage item On root media, cuttage depth is 1-1.5cm, and IBA of the mass-volume concentration for 0.1mg/L is used before cuttage for cuttage Dipping, and after cuttage, controlled at 24-26 DEG C, intensity of illumination 1000-2000LX, light application time are 15-17h/ days, training It supports two months, you can;
It is that the plant that plant height is 6-8cm is transferred in root media that the culture in glassware, which is taken root, wherein root media It is to be contained in wide-mouth bottle, root media adds IBA for 1/2WPM culture mediums so that the concentration of IBA in the medium is 0.1mg/L, then place it in that temperature is 24-26 DEG C, intensity of illumination 1000-2000LX, light application time are 15-17h/ days, training It supports two months, you can.
2. blueberry method for culturing seedlings as described in claim 1, which is characterized in that the root media is the outer cuttage root-taking of bottle Culture medium, consisting of peat soil and bark powder are 3 according to mass ratio:1 carries out uniformly mixed mixture.
3. blueberry method for culturing seedlings as described in claim 1, which is characterized in that the sterile water is distilled water or tap water quilt 80-100 DEG C is boiled 10-30min postcoolings to the cooling water of room temperature.
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